Back to PHM 309

Study notes

Written and reviewed by subject experts from the same material the questions were written from. Read a note, then practise the questions it teaches.

Notes on 81 of 95 objectives.

Pharmacology

12 mins read · 12 questions

Explain drug specificity, selectivity, structure–activity relationships and stereoselectivity.

10 mins read · 15 questions

Describe the four receptor superfamilies (ligand-gated ion channels, G protein-coupled receptors, kinase-linked receptors, nuclear receptors): structure, time scale of response and a prototype example of each.

10 mins read · 17 questions

Explain the G-protein cycle and the main effector pathways: Gs/Gi–adenylyl cyclase–cAMP–protein kinase A; Gq–phospholipase C–IP₃/DAG–Ca²⁺–protein kinase C; direct regulation of ion channels.

11 mins read · 14 questions

Describe the second messengers (cAMP, cGMP, IP₅, DAG, Ca²⁺, nitric oxide) and explain signal amplification.

9 mins read · 14 questions

Apply the law of mass action and occupancy theory (Hill–Langmuir equation) to relate drug concentration to receptor occupancy.

9 mins read · 13 questions

Define and distinguish affinity (KA/Kd), efficacy (intrinsic activity), potency (EC₅₀) and maximal effect (Emax).

12 mins read · 9 questions

Construct and interpret graded concentration–response curves (arithmetic and log scale) and quantal dose–response curves (ED₅₀, TD₅₀, LD₅₀, therapeutic index, margin of safety).

12 mins read · 14 questions

Distinguish full agonists, partial agonists, inverse agonists and neutral antagonists; explain constitutive receptor activity.

10 mins read · 11 questions

Explain spare receptors (receptor reserve) and their effect on agonist potency and on the action of irreversible antagonists.

11 mins read · 14 questions

Classify antagonism: reversible competitive, irreversible (non-equilibrium) competitive, non-competitive, allosteric, chemical, pharmacokinetic and physiological (functional), with an example of each.

11 mins read · 14 questions

Predict the effect of each type of antagonist on an agonist concentration–response curve (parallel rightward shift versus depression of the maximum).

12 mins read · 9 questions

Explain the behaviour of a partial agonist given alone and in the presence of a full agonist.

Get the course to read them

Find your course

Type your course code or its title. We show you exactly what we hold for it.

Or browse by programme